US5165915A - Spherical clay mineral powder, process for production thereof and composition containing the same - Google Patents

Spherical clay mineral powder, process for production thereof and composition containing the same Download PDF

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US5165915A
US5165915A US07/538,595 US53859590A US5165915A US 5165915 A US5165915 A US 5165915A US 53859590 A US53859590 A US 53859590A US 5165915 A US5165915 A US 5165915A
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powder
water
clay mineral
spherical
organic
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Inventor
Kazuo Tokubo
Michihiro Yamaguchi
Jyunko Suzuki
Toshio Yoshioka
Fujihiro Kanda
Minoru Fukuda
Toshihide Ikeda
Takeshi Kawaura
Yoshiaki Yagita
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Shiseido Co Ltd
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Shiseido Co Ltd
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Priority claimed from JP61174578A external-priority patent/JPH0696447B2/ja
Priority claimed from JP61188333A external-priority patent/JPS6343665A/ja
Priority claimed from JP61194493A external-priority patent/JPH075292B2/ja
Priority claimed from JP19449486A external-priority patent/JPS6351310A/ja
Priority claimed from JP20862486A external-priority patent/JPH0662288B2/ja
Priority claimed from JP61209161A external-priority patent/JPH0717371B2/ja
Priority claimed from JP20916086A external-priority patent/JPS6366111A/ja
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26—Aluminium; Compounds thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0216—Solid or semisolid forms
    • A61K8/022—Powders; Compacted Powders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241—Containing particulates characterized by their shape and/or structure
    • A61K8/025—Explicitly spheroidal or spherical shape
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06—Lipsticks
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/08—Preparations containing skin colorants, e.g. pigments for cheeks, e.g. rouge
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/12—Face or body powders for grooming, adorning or absorbing
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00—Anti-perspirants or body deodorants
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/0081—Composite particulate pigments or fillers, i.e. containing at least two solid phases, except those consisting of coated particles of one compound
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/40—Compounds of aluminium
    • C09C1/42—Clays
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/01—Particle morphology depicted by an image
    • C01P2004/03—Particle morphology depicted by an image obtained by SEM
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/30—Particle morphology extending in three dimensions
    • C01P2004/32—Spheres
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/60—Particles characterised by their size
    • C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/12—Surface area
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S424/00—Drug, bio-affecting and body treating compositions
    • Y10S424/05—Stick

Definitions

  • the present invention relates to a spherical clay mineral powder or spherical composite powder comprising a water-swellable clay mineral with a specific surface area of 100 m 2 /g or more, a process for production thereof, and a composition containing the same.
  • These spherical clay mineral powders are suitable as a filler in rubbers, plastics, etc., due to their excellent moldability, and as a powder for use in cosmetics and pharmaceuticals, due to their excellent tactility.
  • specific surface area is a BET method value determined from the nitrogen adsorption amount at the liquid nitrogen temperature, and in water-swellable clay mineral, refers to the value corresponding to the outer surface area including the end surfaces, because no nitrogen molecule has penetrated between the layers at the liquid nitrogen temperature.
  • the swelling and gelling characteristics of a water-swellable clay mineral have enabled its use as a dispersing stabilizer for paints, pharmaceuticals, cosmetics and it is also utilized in powder form as a filler for plastics, rubbers, and the like. Particularly when utilized in the powdery form, whether a natural or a synthetic product, it is finally reduced to powder by mechanical pulverization, and therefore, most particles have an indefinite form and thus a poor efficiency when used as a filler, and can be formulated only with difficulty in cosmetics, in which importance form characteristic gives a gritty touch.
  • powders have surface activities, and thus will frequently cause a deterioration of co-existing components in pharmaceutical, food, cosmetic, paint, etc., systems.
  • a composite powder has been formed by coating the powder surface with another powder by utilizing, for example, a sand mill.
  • the powder covering the powder surface may also cause deterioration.
  • a water-swellable clay mineral undergoes interlayer reaction with organic polar molecules or cationic molecules of alcohol, amine, water-soluble polymer, etc., to form an organic composite clay mineral having a new function.
  • organic composite clay mineral is taken out in powdery form, generally the steps of filtration or centrifugation are employed and after drying of the precipitate, pulverization with a strong mechanical force, whereby most of the particulate forms obtained exhibit an indefinite form, and therefore, the feeling during use has an extremely gritty touch, and thus the drawback arises that they can be formulated only with difficulty into cosmetics in which importance is attached to tactility, except for a formulation when swollen or when dispersed in an aqueous solvent.
  • an emollient agent has been frequently formulated, but this has a drawback of a sticky feeling during use when formulated in a large amount.
  • An oil-soluble dye typically a natural dye, involves a problem of light resistance, and the like, and has a drawback in that it may be dissolved into oil when used as a pigment when formulated in a powdery product or that, due to a weak coloration, the powder must be formulated in a large amount, thus raising costs and having a poor useability.
  • Some of the perfumes have a drawback in that the aroma becomes weaker with an elapse of time, and that a uniform mixing can be done only with difficulty when a perfume is given to a product consisting only of powder.
  • water-soluble substances typically polyhydric alcohol
  • these water-soluble substances have an excellent humectant action, they also have a drawback of a sticky feeling during use when formulated in a large amount.
  • a liquid water-soluble substance has a drawback in that it can be formulated in a powdered cosmetic such as pressed powder only with difficulty.
  • a water-swellable clay mineral has been used as the dispersing stabilizer for paints, pharmaceuticals, and cosmetics by utilizing its swellability, gelling characteristic, since it has a particularly high stability and good gelling ability, and therefore, is preferable for use in cosmetics, above all in a powder dispersion system or emulsified system product (e.g., eyeliner, mascara, emulsion, cream, nail enamel).
  • a powder dispersion system or emulsified system product e.g., eyeliner, mascara, emulsion, cream, nail enamel.
  • it is formulated in the form of a gel dispersed in an aqueous solvent.
  • the formulation of the powdery form as such directly into a cosmetic is rarely practiced, but even if formulated directly in the powdery form, due to its indefinite form, a gritty feeling occurs during use, and therefore, it can be formulated only with difficulty into a cosmetic in which importance is attached particularly to the feeling during use.
  • an object of the present invention is to solve the problems of the prior art as described above, in the making of the water-swellable clay mineral spherical powder, and the like, because the spherical clay mineral powder having an excellent filling efficiency and an excellent feeling during use.
  • Another object of the present invention is to provide a composite powder which is also stable in various systems by enclosing the surface activity of the desired powder by incorporating one or two or more kinds of organic, inorganic or metallic powder or inorganic sol-like substance in a powder comprising water-swellable clay mineral without impairing the function of the desired powder.
  • Still another object of the present invention is to provide a composite powder, which is a spherical organic composite clay mineral powder containing a water-swellable clay mineral and an organic substance soluble in an organic solvent and, when the organic substance is an emollient agent, has a moist feeling during use and an excellent emollient effect without stickiness even when formulated in a large amount, or when the organic substance is an oil-soluble dye, has an excellent light resistance and coloration power, or when the organic substance is a perfume, has an excellent safety and slow release property, giving in all cases, a smooth feeling during use due to the spherical shape, and further, can be stably formulated in powdery cosmetics.
  • Still another object of the present invention is to provide an excellent spherical composite powder which is an organic composite clay mineral comprising a water-swellable clay mineral and a water-soluble substance, having a smooth and moist feeling during use as well as an excellent humectant action, without stickiness even when formulated in a large amount, and further, can be formulated stably in powdery cosmetics.
  • Still another object of the present invention is to make a water-swellable clay mineral spherical, which can be formulated in a cosmetic, thereby providing a cosmetic having a transparency and good feeling during use, such as slippage, etc.
  • Still another object of the present invention is to provide a deodorant with a good safety and good useability and having a truly excellent deodorizing effect which persists for a long time, in view of the state of the prior art deodorant of an insufficient deodorizing effect, non-persistency of the effect or unsatisfactory local application, safety and useability.
  • the spherical clay mineral powder according to the present invention comprises a water-swellable clay mineral with a specific surface area of 100 m 2 /g or more, and the water-swellable spherical clay mineral powder can be produced by dispersing a water-swellable clay mineral with a specific surface area of 100 m 2 /g or more in an aqueous dispersion, and then spray drying the dispersion.
  • a spherical composite powder containing one kind or two kinds or more of organic, inorganic or metallic powder or inorganic sol-like substance in powder comprising a water-swellable clay mineral with a specific surface area of 100 m 2 /g or more, which composite powder can be prepared by spray drying one kind or two or more kinds of organic, inorganic or metallic powder or inorganic sol-like substance and an aqueous dispersion of the water-swellable clay mineral.
  • an organic composite clay mineral powder containing a water-swellable clay mineral with a specific surface area of 100 m 2 /g or more and an organic substance soluble in an organic solvent.
  • an organic composite clay mineral, powder containing a water-swellable clay mineral with a specific surface area of 100 m 2 /g or more and a water-soluble substance containing a water-swellable clay mineral with a specific surface area of 100 m 2 /g or more and a water-soluble substance.
  • a deodorant comprising a composite powder comprising a water-swellable clay mineral and powder having a deodorizing activity
  • its embodiments are inclusive of deodorants for external use such as an aerosol, roll-on, powder, cream, stick, and for modes such as a lining sheet in shoes and deodorants for domestic use.
  • FIG. 1 is a scanning electron microscope photograph ( ⁇ 10,000) showing the crystalline structure of the spherical clay mineral powder according to the present invention obtained in Example 1;
  • FIG. 2 is a scanning electron microscope photograph showing the crystalline structure of the spherical composite powder of the present invention containing 25% by weight of fine particulate titanium dioxide obtained in Example 7;
  • FIG. 3 shows UV-rays absorption curves of the composite powder of the present invention dispersed in castor oil (containing fine particulate titanium dioxide) and fine particulate titanium dioxide alone dispersed similarly in castor oil (curve (a): the composite powder of the present invention, curve (b): fine particulate titanium dioxide alone);
  • FIG. 4 is a scanning electron microscope photograph showing the spherical composite powder of the present invention containing the perfume component citral obtained in Example 13;
  • FIG. 5 is a scanning electron microscope photograph showing the composite powder obtained in Example 26.
  • the water-swellable clay mineral to be used in the present invention may include water-swellable clay minerals with a specific surface area of 100 m 2 /g or more, preferably 150 m 2 /g or more, particularly synthetic layered silicate minerals such as hectorite or saponite.
  • water-swellable clay minerals for example, commercially available products such as Laponite (Laporte Co.), Smecton SA (Kunimine Kogyo), etc. can be suitably used.
  • "water-swellable" clay mineral means a layered silicate mineral which becomes a uniform gel which is approximately transparent when dispersed in water.
  • the spherical clay mineral powder according to the present invention can be most simply prepared by the spray drying method according to, for example, the present invention, whereby a spherical powder with regular particle forms and particles sizes can be obtained.
  • a water-swellable clay mineral with a specific surface area of 100 m 2 /g or more is dispersed in an aqueous medium to be gelled, and then the dispersion is spray dried.
  • the concentration of the water-swellable clay mineral is controlled to not higher than 20% by weight, particularly desirably, 1 to 10% by weight.
  • concentration exceeding 20% by weight the gel viscosity is higher, whereby delivery of the liquid to a spraying nozzle at the time of spray drying is very difficult, and clogging of the nozzle, etc. may occur.
  • stirring is performed until the water-swellable clay mineral is sufficiently dispersed and swollen.
  • clogging of the nozzle during spray drying may occur, or in some cases, the spherical clay mineral may become undesirably irregular.
  • the inlet air temperature during spraying can be set at a broad temperature range of about 150° to 300° C.
  • the exhaust temperature may be defined depending on the spray flow rate from the nozzle, etc., but may be around approximately 100° C.
  • the spherical clay mineral may have a particle size of 2 to 30 ⁇ m. Also, the form of the particle surface becomes uniform and smooth, as the appearance of the above gel is more transparent and has a higher viscosity (for example, in the case of Laponite).
  • the spherical clay mineral obtained as described above is then calcined, if desired.
  • the calcination temperature, the calcination time and the atmosphere for calcination may be selected depending on the use, but the calcination temperature must not be higher than the temperature at which mutual sintering occurs between the spherical clay minerals. This temperature is about 900° C. or higher. At a calcination temperature range lower than that temperature, a change in crystalline structure by X-ray diffraction measurement may sometimes occur, but this is not a problem if the shape remains spherical. The particle size will not be substantially changed by calcination.
  • Formulation of the spherical clay mineral according to the present invention into a cosmetic is possible in all concentration ranges, and is generally 0.05% to 50% by weight.
  • concentration ranges is generally 0.05% to 50% by weight.
  • a concentration ranging from 0.5% to 5% by weight is general, and in the case of powdery or powder pressed type, a concentration ranging from 0.1% to 30% by weight is general.
  • components generally formulated in cosmetics can be formulated within the qualitative, quantitative ranges which do not impair the present invention.
  • examples of such components are oil components, waxes, pigments, powders, surfactants, preservatives, dyes, antioxidants, UV-ray absorbers, perfumes, humectants such as polyhydric alcohols, chelating agents, acids, alkalis, water-soluble polymers, oil-soluble polymers, clay minerals.
  • oil components waxes, pigments, surfactants are enumerated below.
  • Waxes and oil components animal and vegetable oils such as tallow, squalene olive oil, evening primrose oil, rice bran oil, candelilla wax, carnauba wax, mineral oils such as hydrocarbons, fluid paraffins, solid paraffins; ester oils such as isopropyl myristate, pentaerhtritol-tetra-2-ethylhexanoate, silicone oils such as methylphenylsilicone, dimethylsilicone; alcohols such as 2-octyldodecanol, 2-decyltetradecanol, oleyl alcohol, cetyl alcohol; fatty acids such as behenic acid, oleic acid, isostearic acid; and, higher alcohols such as oleyl alcohol, cetanol, stearyl alcohol.
  • animal and vegetable oils such as tallow, squalene olive oil, evening primrose oil, rice bran oil, candelilla wax, carnauba wax, mineral oils such
  • nonionic surfactants including polyoxyethylene (hereinafter abbreviated as POE)-branched alkyl ethers such as POE-octyldodecyl alcohol, POE-2-decyltetradecyl alcohol; POE-alkyl ethers such as POE-oleyl alcohol ether, POE-cetyl alcohol ether; sorbitan esters such as sorbitan monooleate, sorbitan monoisostearate, sorbitan monolaurate; POE-sorbitan esters such as POE-sorbitan monooleate, POE-sorbitan monoisostearate, POE-sorbitan monolaurate; glycerine fatty acid esters such as glycerine monooleate, glyceryl monostearate, glyceryl monomyristate; POE-glycerine fatty acid esters such as POE-glyceryl monooleate, POE-gly
  • Pigments inorganic pigments such as talc, mica, kaolin, calcium carbonate, zinc white, titanium dioxide, red iron oxide, yellow iron oxide, black iron oxide, ultramarine, prussian blue, chromium hydroxide, titanium coated mica, bismuth oxychloride; organic pigments such as crystalline cellulose, nylon powder, polyethylene powder.
  • inorganic pigments such as talc, mica, kaolin, calcium carbonate, zinc white, titanium dioxide, red iron oxide, yellow iron oxide, black iron oxide, ultramarine, prussian blue, chromium hydroxide, titanium coated mica, bismuth oxychloride
  • organic pigments such as crystalline cellulose, nylon powder, polyethylene powder.
  • any organic, inorganic or metal powder or inorganic sol-like substance can be used as the powder to be contained in the powder comprising the water-swellable clay mineral of the present invention.
  • Representative examples may include organic powder such as of polyamide resin, polyethylene resin, acrylic resin, polyester resin, fluorine resin and cellulose resin; inorganic powder such as of titanium dioxide, talc, kaolin, hydroxyapatite, zinc white, barium sulfate, magnesium carbonate, calcium carbonate, silica, calcium secondary phosphate, iron oxide, chromium oxide, chromium hydroxide, ultramarine, prussian blue; metallic powder such as aluminum powder, gold powder, silver powder, iron powder, copper powder, zinc powder; and inorganic sol-like substance such as silica sol, alumina sol, titania sol, zirconia sol.
  • organic powder such as of polyamide resin, polyethylene resin, acrylic resin, polyester resin, fluorine resin and cellulose resin
  • inorganic powder such as of titanium dioxide, talc, kaolin, hydroxyapatite, zinc white, barium sulfate, magnesium carbonate, calcium carbonate, silica, calcium secondary phosphate, iron oxide,
  • the particle size of the above organic, inorganic or metallic powder should be preferably 0.5 ⁇ m or less in average particle diameter, particularly 0.1 ⁇ m or less, since the composite powder constituted of the water-swellable clay mineral and these powders has a particle size of about 2 to 30 ⁇ m. If the size is greater than this, the above powder to be contained within the powder of the water-swellable clay mineral will undesirably appear frequently on the surface of the composite material.
  • the content of the organic, inorganic or metallic powder or the inorganic sol-like substance in the composite powder comprising the water-swellable clay mineral and one kind or two or more kinds of the organic, inorganic or metallic powder or the inorganic sol-like substance may be 0.1% to 100% by weight of the total amount of the composite powder.
  • the particle size of the composite powder comprising the water-swellable clay mineral and one kind or two or more kinds of the organic, inorganic or metallic powder or the inorganic sol-like substance is 2 to 30 ⁇ m on an average.
  • the composite powder may have any desired shape, but particularly when formulated into a product to which the feeling during use is important, such as cosmetics, etc., it should be preferably approximately spherical. To obtain a spherical composite powder, the following preparation process according to the present invention is most preferable.
  • one kind or two or more kinds of organic, inorganic or metallic powder or inorganic gel-like substance to be contained is dispersed in an aqueous solvent.
  • various surfactants or dispersing agents such as sodium hexametaphosphate may be added.
  • a water-swellable clay mineral is added to this dispersion to prepare a gel. It is important that one kind or two or more kinds of the above organic, inorganic or metallic powder or inorganic gel-like substance be uniformly dispersed in the gel.
  • the dispersion thus obtained is spray dried, whereby water jetted out from the nozzle is instantly evaporated to give the composite powder of the present invention.
  • the obtained composite powder is spherical.
  • the concentration of the water-swellable clay mineral in the above gel preferably is 10% by weight or less. At a concentration exceeding this level, the gel viscosity becomes too high, whereby delivery of the liquid to the spraying nozzle during spray drying is difficult, and clogging of the nozzle or the like is liable to occur.
  • the content of one kind or two or more kinds of the organic, inorganic or metallic powder may be determined so that the weight in the total weight of the composite powder after drying may be within the above range.
  • a general spray drying method such as disc type, pressure nozzle system, 2-fluid nozzle system, etc. can be applied.
  • the inlet air temperature during spraying which also depends on the stability of the one kind or two or more kinds of the organic, inorganic or metallic powder, can be set at a broad temperature range of about 100° to 300° C., because the water-swellable clay mineral is thermally stable up to about 300° C.
  • the exhaust temperature may differ depending on the spraying flow rate from the nozzle, but may be generally around 100° C.
  • the spherical clay mineral thus obtained has a particle size of 2 to 30 ⁇ m, and exhibits a spherical shape.
  • the particle surface becomes more uniform and smooth as the appearance of the gel prepared is more transparent, and the viscosity of the gel is higher (for example, in the case of Laponite).
  • the composite powder of the present invention thus obtained has a particle size of about 2 to 30 ⁇ m on an average, although this can slightly differ depending on the spray drying conditions.
  • the spherical composite powder obtained above is then calcined, if desired.
  • the calcination temperature, the calcination time, and the atmosphere for calcination may be selected depending on the use, but the calcination temperature must not be higher than the temperature at which a mutual sintering occurs between spherical clay minerals. This temperature is about 900° C. or higher. At a calcination temperature lower than that temperature, a change in crystalline structure may be sometimes occur, but this is not a problem if the shape remains spherical.
  • the particle size of the spherical composite powder thus obtained is not substantially changed by calcination, but the water absorptivity of the spherical powder is reduced by calcination, and further, the water swellability is lost.
  • the organic substance soluble in an organic solvent to be used in the present invention is a substance insoluble in water, including specific oil components having an emollient effect, oil-soluble dyes, perfumes, UV-rays absorbers.
  • oil component having the emollient effect may include isopropyl myristate, myristyl lactate, dipentaerythritol fatty acid ester, glycerine trimyristate, alkylene glycol fatty acid ester.
  • oil-soluble dye examples include tar dyes such as red color No. 215, red color No. 218, red color No. 223, red color No. 225, orange color 201, yellow color 204, green color 202, violet color 201, etc., natural dyes such as B-carotene, annatto, sakuro-high yellow, carmic acid, etc.
  • tar dyes such as red color No. 215, red color No. 218, red color No. 223, red color No. 225, orange color 201, yellow color 204, green color 202, violet color 201, etc.
  • natural dyes such as B-carotene, annatto, sakuro-high yellow, carmic acid, etc.
  • perfume examples include linalol, linalyl acetate, cinnamic aldehyde, benzyl acetate, citral, cimene, limonene, etc.
  • Example of the UV-rays absorber may include paraaminobenzoic acid, homomenthyl-N-acetylanthranilate, anilsalicylate, octylsalicylate, 2,4-dihydroxybenzophenone.
  • the organic composite clay mineral of the present invention is a spherical powder containing the above water-swellable clay mineral and an organic substance soluble in an organic solvent, having a particle size of 2 to 30 ⁇ m.
  • the amount of the water-swellable clay mineral formulated in the total amount of the organic composite clay mineral may be 25% to 99.5% by weight, preferably 50% to 99.9% by weight, and the amount of the organic substance soluble in an organic solvent formulated in the total amount of the organic composite clay mineral may be 0.05% to 75% by weight, preferably 0.1% to 50% by weight.
  • the organic composite clay mineral of the present invention may be prepared according to any desired process, but the following spray drying process is the simplest and most preferable for obtaining an organic composite clay mineral with a regular spherical shape.
  • the water-swellable clay mineral is dispersed in an aqueous solvent to be gelled, and then the spherical water-swellable clay mineral is obtained by spray drying of the gel.
  • the concentration of the water-swellable clay mineral in the above gel may be preferably 10% by weight or less. At a concentration higher than that level, the gel viscosity becomes, too high, whereby delivery of the liquid to the spraying nozzle during spraying is difficult, and clogging of the nozzle or the like may be occur.
  • a particularly preferable concentration range is 1% to 10% by weight.
  • stirring is performed until the water-swellable clay mineral is sufficiently dispersed and swelled.
  • clogging of the nozzle during spray drying may occur, or in some cases, the organic composite clay minerals obtained may become undesirably irregular.
  • a general spray drying method such as disc type, pressure nozzle system, 2-fluid nozzle system, may be applied.
  • the inlet air temperature during spraying is preferably in the temperature range at which the swellable clay mineral is thermally stable, and may be about 150° to 300° C.
  • the exhaust temperature may be defined depending on the spray flow rate from the nozzle or the like, but may be around 100° C.
  • the clay mineral thus obtained is a substantially truly spherical powder having a structure comprising primary particles of water-soluble clay mineral agglomerated, having a particle size of 2 to 30 ⁇ m.
  • the form of the particle surface becomes more uniform and smooth as the appearance of the gel previously formed is more transparent and the viscosity is higher (for example, in the case of Laponite).
  • the spherical water-swellable clay mineral thus obtained is dispersed in an organic solvent containing the above organic substance dissolved therein, and thereafter, the organic solvent is volatilized.
  • the organic solvent to be used may be any general low boiling solvent, as exemplified by methanol, ethanol, chloroform, ether, hexane and the like.
  • the organic substance dissolved in an organic solvent according to such operations is included as permeated between the layers of spherical water-swellable clay mineral to give a spherical organic composite clay mineral.
  • the spherical water-swellable clay mineral is not swollen in an organic solvent, and therefore, its shape is not changed.
  • the organic composite clay mineral thus obtained maintains its original shape.
  • the water-soluble substance to be used in the present invention is any desired water-soluble substance, including muco-polysaccharides such as hyaluronic acid, chondroitin sulfuric acid A, chondroitin sulfuric acid B, chondroitin sulfuric acid C, heparin sulfuric acid, heparin keratin sulfuric acid; natural water-soluble polymers, for example, vegetable polymers such as gum arabic, gum tragacanth, galactane, guar gum, carob gum, karaya gum, caragheenan, pectin, agar, quince seed (marmelo), algae colloid (brown algae extract), starch (rice, corn, potato, wheat); microorganism polymers such as xanthan gum, dextran, succinoglucan, pullulane, semi-synthetic water-soluble polymers, for example, starch polymers such as carboxymethyl starch, methlhydroxypropyl starch, cellulose polymers such as methylcellulose, nitrocellulose,
  • polyhydric alcohols and mucopolysaccharides are particularly desirable.
  • one or two or more kinds are selected as desired from these water-soluble substances.
  • the organic composite clay mineral of the present invention is a spherical powder containing the above water-swellable clay mineral and a water-soluble substance, and having a particle size of 2 to 30 ⁇ m.
  • the amount of the water-swellable clay mineral formulated in the total amount of the organic composite clay mineral may be 25% to 99.5% by weight, preferably 50% to 99.9% by weight, and the amount of the water-soluble substance formulated in the total amount of the organic composite clay mineral may be 0.05% to 75% by weight, preferably 0.1% to 50% by weight.
  • the organic composite clay mineral of the present invention may be prepared according to any desired process, but the following spray drying process is the simplest and most preferable for obtaining an organic composite clay mineral with a regular spherical shape.
  • the above water-soluble substance is dissolved in an aqueous solvent, and further, the above water-swellable clay mineral is dispersed therein to be gelled, and then the gel can be spray dried to obtain an organic composite mineral containing a water-swellable clay mineral and a water-soluble substance.
  • the concentration of the water-swellable clay mineral in the above gel containing the water-soluble substance and the water-swellable mineral may be preferably 20% by weight or less. At a concentration higher than that level, the gel viscosity becomes too high, whereby delivery of the liquid to the spraying nozzle during spraying is difficult, and also clogging of the nozzle may occur.
  • a particularly preferable concentration range is 1% to 10% by weight.
  • the concentration of the water-soluble substance in the above gel may be preferably 0.001% to 5% by weight. At a concentration more than this range, a water-soluble substance which cannot be included within the organic composite clay mineral also appears, whereby the amount of the water-soluble substance adsorbed on the organic composite clay mineral surface may be increased to give an undesirable sticky feeling during use or effect powdering of the water-soluble substance alone.
  • stirring is performed until the water-swellable clay mineral is sufficiently dispersed and swollen.
  • clogging of the nozzle during spray drying may occur, or in some cases, the organic composite clay minerals obtained may become undesirably irregular.
  • a general spray drying method such as disc type, pressure nozzle system, 2-fluid nozzle system, etc., may be applied.
  • the inlet air temperature during spraying is preferably in the temperature range where the swellable clay mineral is thermally stable, and may be about 100° to 200° C.
  • the exhaust temperature may be defined depending on the spray flow rate from the nozzle or the like, but may be around 100° C.
  • the clay mineral thus obtained is a substantially truly spherical powder having a structure comprising primary particles of water-soluble clay mineral agglomerated, having a particle size of 2 to 30 ⁇ m.
  • the form of the particle surface becomes more uniform and smooth, as the appearance of the gel previously formed is more transparent and the viscosity is higher (for example, in the case of Laponite).
  • the polyhydric alcohol is included between the layers of the water-swellable clay mineral. This can be confirmed by expansion of the longer interplaner spacing in X-ray diffraction.
  • a muco-polysaccharide When a muco-polysaccharide, is selected as the water-soluble substance, this will-not penetrate between the layers of clay mineral, but is included with the organic composite clay mineral in the form adsorbed on the primary particle surface of the water-swellable clay mineral.
  • the water-soluble substance is soluble in an organic solvent other than water
  • a method for preparation of such a spherical organic composite clay mineral a method is known in which spherical clay mineral is prepared and, thereafter, a water-soluble substance is permeated therethrough. More specifically, by spray drying a water-dispersed gel Only of the water-swellable clay mineral, a spherical clay mineral containing no water-soluble substance is obtained. By dispersing this in an organic solvent containing a water-soluble substance previously dissolved therein, and thereafter volatilizing the organic solvent, the water-soluble substance will be included in the spherical clay mineral dispersed.
  • the spherical organic composite clay mineral thus prepared becomes entirely the same powder as the powder obtained by spray drying of a water-dispersed gel previously containing the water-soluble substance and the water-swellable clay mineral dispersed therein.
  • the organic solvent used at this time may be a low boiling solvent.
  • methanol, ethanol, acetone, chloroform, ether, and hexane can be utilized.
  • the water-soluble substance soluble in organic solvent polyhydric alcohols, quaternary ammonium salts, etc. may be included.
  • the amount of the spherical organic clay mineral formulated in cosmetic may be as desired depending on the form of the cosmetic, ranging generally from 0.1% to 80% by weight. In the case of an emulsified, dispersed system, it is generally 0.1% to 50% by weight, and is generally 0.1% to 70% by weight in the case of powdery or powdery pressed type products.
  • components generally formulated in cosmetics can be formulated within the qualitative and quantitative ranges which do not impair the effect of the present invention.
  • Such components may include oil components, waxes, pigments, powders, surfactants, preservatives, dyes, antioxidants, UV-rays absorbers, perfumes, humectants such as polyhydric alcohols, chelating agents, acids, alkalis, water-soluble polymers, oil-soluble polymers, clay minerals.
  • the powder having a deodorizing activity to be used in the present invention may include metal oxides such as zinc oxide, magnesium oxide, calcium oxide, hydroxyapatite, activated charcoal, zeolite, metal phthalocyanine, glycine metal complex, particularly preferably, zinc oxide.
  • metal oxides such as zinc oxide, magnesium oxide, calcium oxide, hydroxyapatite, activated charcoal, zeolite, metal phthalocyanine, glycine metal complex, particularly preferably, zinc oxide.
  • any desired one kind or two or more kinds from among these can be selected to be used.
  • the deodorant of the present invention contains a composite powder comprising the above water-swellable clay mineral and the above powder has a deodorizing activity.
  • This composite powder may be preferably in the state in which the powder having a deodorizing activity is embedded internally in the water-swellable clay mineral.
  • the structure of the composite powder has a multitude of fine pores in the form in which primary particles of the water-swellable clay mineral are gathered together, and therefore, bad odor components which are gaseous are partially trapped in fine pores, a part thereof penetrating into the inner portion of the powder to be deodorized through the reaction with the powder having a deodorizing activity in the inner portion of the powder.
  • Such a composite powder may be specifically prepared by dispersing the powder having a deodorizing activity and the water-swellable clay mineral in an aqueous solvent to prepare a gel containing the powder having a deodorizing activity well dispersed therein, and then drying the gel.
  • an activator or a dispersing agent such as sodium hexametaphosphate also may be added.
  • the method for drying the gel there may be included drying by applying heat, freeze drying, spray drying, or the like, of which spray drying is particularly preferred.
  • spray drying of the gel the aqueous solvent from the droplets of the aqueous solvent jetted out from the nozzle is rapidly evaporated to give a composite powder.
  • the composite powder thus obtained is spherical and about 2 to 30 ⁇ m, and therefore, the deodorant has the specific feature of being useable with an extremely good slippage in the roll-on, powder, cream, stick type, without clogging from the nozzle in the aerosol type.
  • the constitutional ratio of the water-swellable clay mineral to the powder having a deodorizing activity can be freely changed depending on the product form and is not particularly limited, but preferably the weight ratio of the powder having a deodorizing activity based on the water-swellable clay mineral is 2% to 60%. With a ratio less than 2%, the deodorizing effect may not be exhibited, and with a ratio exceeding 60%, the powder having a deodorizing activity may appear frequently on the composite powder surface, whereby the merit of composite formation may be lost.
  • the particle size of the composite powder may be preferably about 2 to 30 ⁇ m in average diameter, with the average particle size of the powder having a deodorizing activity being desirably 0.01 to 0.5 ⁇ m, preferably 0.1 ⁇ m or less.
  • the composition of the gel may be preferably prepared to a concentration of 0.5% to 10% by weight of the water-swellable clay mineral. At a concentration exceeding 10% by weight, the gel viscosity is too high, whereby delivery of the liquid to the spraying nozzle during spray drying becomes difficult, and clogging of the nozzle, etc. is liable to occur.
  • a general spray drying method such as disc type, pressure nozzle system, or 2-fluid nozzle system may be applied.
  • the inlet air temperature which may also depend on the stability of the powder having deodorizing activity, can be set at a wide temperature range of 100° to 300° C., because the water-swellable clay mineral is thermally stable up to 300° C.
  • the exhaust temperature is limited depending on the spray flow rate from the nozzle, but may be generally around 100° C.
  • the composite powder When the composite powder is prepared by drying the gel of the water-swellable clay mineral and the gel of the powder having a deodorizing activity, the form of the particle surface becomes more uniform and smooth, as the appearance of the gel previously prepared is more transparent and higher in viscosity (for example, in the case of Laponite).
  • the deodorant comprising the composite powder according to the present invention has an excellent deodorizing effect, and may be contained in a deodorant for external use such as an aerosol, roll-on, powder, cream, stick, or deodorants in the form of a base lining for shoes and domestic uses in an amount of 0.1% to 100% by weight. With an amount less than 0.1% by weight, the deodorizing effect can be exhibited only with difficulty.
  • any desired component known in the art can be formulated into the above essential components. Also, together with said composite powder, it is possible to formulate any component known in the art in the deodorant for external use such as an aerosol, roll-on, powder, cream, stick, or base lining of shoes and deodorants for domestic use.
  • oils and fats such as avocado oil, almond oil, olive oil, grape seed oil, sesame oil, sasanqua oil, safflower oil, soybean oil, camellia oil, corn oil, rapeseed oil, persic oil, castor oil, sunflower oil, cottonseed oil, peanut oil, cacao oil, palm oil, coconut oil, tallow, fish fat, hardened oil, turtle oil, pig oil, mink oil, yolk oil; waxes such as whale wax, shellac, beeswax, lanolin, liquid lanolin, carunauba wax, canderilla wax; hydrocarbons such as fluid paraffin, fluid polyisobutylene, squalene, pristane, petrolatum, paraffin, ceresin; fatty acids such as succinic acid, tartaric acid, citric acid, undecylenic acid, lauric acid, myristic acid, palmitic acid, stearic acid, isostearic acid, o
  • red color 202 yellow color 201, green color 204, violet color 201
  • inorganic dyes such as aluminum powder, talc, kaolin, bentonite, mica, mica titanium, red iron oxide, caramine, etc.
  • UV-ray absorbers such as urocanic acid, cinoxate
  • antiphlogistic agents such as allantoin, aloe powder, guayzulene
  • propellants such as Freon 11, Freon 12, Freon 21, Freon 22, Freon 113, Freon 114, Freon C318, methyl chloride, methylene chloride, isobutane, carbon dioxide; and purified water.
  • Other additives which can be optionally formulated in the deodorant according to the present invention may include, for example, sweat inhibitors such as aluminum hydroxychloride, aluminum chloride, aluminum sulfate, basic aluminum bromide, aluminum phenolsulfonic acid, tannic acid, aluminum naphthalenesulfonic acid, basic aluminum iodide, sterilizers such as 3,4,4-trichlorocarbanilide (TCC), benzalkonium chloride, benzethonium chloride, alkyltrimethylammonium chloride, resorcin, phenol, sorbic acid, salicylic acid, hexachlorophene, masking agents such as musk, scatol, lemone oil, lavender oil, jasmine, benzoin, benzyl acetate, menthol.
  • sweat inhibitors such as aluminum hydroxychloride, aluminum chloride, aluminum sulfate, basic aluminum bromide, aluminum phenolsulfonic acid, tannic
  • the spherical clay mineral of the present invention can be an excellent filler with a high molding efficiency in plastics, rubber, etc. since it is spherical, and excellent as a filler for liquid chromatography. Also, when formulated in cosmetics, a cosmetic having an extremely good slippage without a sandy feeling during use can be provided.
  • one kind or two or more kinds of organic, inorganic or metallic powder or inorganic sol-like substance can be also formulated in all bases without reaction with other co-existing components in the system to provide a stable product.
  • the powder is suitable as a filler and has a particularly good filling efficiency.
  • the powder has specific features such that when used in paints, the workability and dispersibility are good, and that the useability is good when used in cosmetics.
  • the spherical organic composite clay mineral is spherical, and therefore, when formulated in cosmetics, gives a smooth and moist feeling during use with an extremely good slippage without a gritty feeling. Also, when the organic substance contained is an oil component having the emollient effect, it is not sticky at all even though having the emollient effect for the skin, having an excellent resistance and coloration power in the case of oil-soluble dye, an excellent stability and slow releasability in the case of a perfume, and further, capable of formulating these substances in any powdered cosmetic.
  • the powder When a humectant is included as the water-soluble substance, the powder exhibits an excellent humectant action for skin, without stickiness, and further, can stably formulate a water-soluble substance in powdered cosmetics.
  • the deodorant comprising the composite powder of the present invention as the effective ingredient has an excellent and persistent deodorizing effect due to the embedding of the powder having a deodorizing activity, and since the powder having a deodorizing activity will not react with other components, the product is not deteriorated, and further, has specific features in that it has an excellent feeling during use with a good slippage and a good safety.
  • Laponite XLG (specific surface area: 330 m 2 /g) was dispersed in 1,000 ml of water while stirring, and the obtained gel was spray dried by a disc spray drying tester at a disc rotational number of 20,000 rpm, an inlet air temperature of about 200° C. and an exhaust temperature of 110° C. As a result, 24 g of spherical powder of 2 to 30 ⁇ m was obtained.
  • FIG. 1 shows a scanning electron microscope photograph of this product.
  • Example 2 An amount of 10 g of spherical Laponite obtained in Example 1 was added to 100 g of polyvinyl chloride powder, and further, tetrahydrofuran was added as the solvent. After stirring, a sheet was prepared, and heated at 80° C. to evaporate tetrahydrofuran, whereby a vinyl chloride sheet was prepared.
  • a vinyl chloride sheet was obtained in the same manner as in Example 2 except for using the commercial product of Laponite XLG which is indefinite in shape as such.
  • the resin composition formulated with the spherical powder of the present invention is a resin composition having an excellent strength.
  • a powdery foundation formulated with the spherical powder obtained in Example 1 was trial-produced according to the following recipe.
  • the numerical values are in % by weight.
  • Powders were charged in a Henschel mixer, uniformly stirred and the remaining components then added and uniformly mixed.
  • the mixture was pulverized by an atomizer and molded in a midplate to obtain a powdery foundation.
  • a powdery foundation was obtained in the same manner as in Example 3 except for using the commercially available Laponite XLG which is indefinite in shape as such.
  • Comparative Example 2 The average score of Comparative Example 2 was 1.9, and the average score of Example 3 was 4.5. Thus, the spherical powder according to the present invention was found to have an extremely good useability when formulated in a foundation.
  • An amount of 30 g of Laponite XLG was dispersed while stirring in 1,000 ml of water.
  • the gel obtained was spray dried by a disc spray drying tester at a disc rotational number of 20,000 rpm, an inlet air temperature of 200° C. and an exhaust temperature of about 100° C., whereby 24 g of 2 to 30 ⁇ m spherical powder was obtained.
  • the spherical powder was calcined at 600° C. for 2 hours.
  • Example 4 An amount of 10 g of the calcined spherical Laponite obtained in Example 4 was added to 100 g of polyvinyl chloride powder, and further tetrahydrofuran was added as the solvent. After the mixture was stirred well, a sheet was prepared and heated at 80° C. to evaporate tetrahydrofuran and prepare a vinyl chloride sheet.
  • a vinyl chloride sheet was obtained in the same manner as in Example 5 except for using the commercial product of Laponite XLG which is indefinite in shape as such.
  • the resin composition formulated with the spherical powder of the present invention is a resin composition having an excellent strength.
  • a powdery foundation formulated with the spherical powder obtained in Example 4 was trial-produced according to the following recipe.
  • the numerical values are in % by weight.
  • Powders were charged in a Henschel mixer, uniformly stirred and the remaining components then added and uniformly mixed.
  • the mixture was pulverized by an atomizer and molded in a midplate to obtain a powdery foundation.
  • a powdery foundation was obtained in the same manner as in Example 3 except for using the commercially available Laponite XLG which is indefinite in shape as such.
  • Example 3 For Example 3 and Comparative Example 2, use tests were conducted by a panel of 20 members.
  • Comparative Example 4 The average score of Comparative Example 4 was 1.9, and the average score of Example 6 was 4.5. Thus, the spherical powder according to the present invention was found to have an extremely good useability when formulated in a foundation.
  • the gel obtained was spray dried by a disc spray drying tester (disc rotational number 20,000 rpm, at an inlet air temperature of about 180° C., and an exhaust temperature of about 110° C.) to obtain 32 g of spherical composite powder of 2 to 15 ⁇ m.
  • FIG. 2 shows a scanning electron microscope photograph of the composite powder. It can be seen that it exhibits a truely spherical shape.
  • the spherical composite powder obtained in Example 7 was dispersed at 10% by weight in castor oil, kneaded thoroughly on three rollers and then applied on a quartz plate by an applicator to a thickness of 5 ⁇ m, followed by measurement of the amount of UV-rays absorbed.
  • fine particulate titanium dioxide not applied with the composite powder formation of the present invention fine particulate titanium dioxide P-25; Degusa Co.
  • fine particulate titanium dioxide P-25 fine particulate titanium dioxide P-25; Degusa Co.
  • the fine particulate titanium dioxide not applied with the composite powder formation of the present invention was dispersed at 2.5% (the same as the amount of particulate titanium dioxide as in Test Example 1) in castor oil, and the amount of UV-rays absorbed was measured as in Test Example 1.
  • the spherical composite powder obtained in Test Example 1 was dispersed at 50% by weight in castor oil, and the degree of odor denaturation of castor oil was measured.
  • fine particulate titanium dioxide not applied with the composite powder formation of the present invention fine particulate titanium dioxide P-25; Degusa Co.
  • fine particulate titanium dioxide P-25 fine particulate titanium dioxide P-25; Degusa Co.
  • the fine particulate titanium dioxide P-25 was dispersed at 2.5% (the same as the amount of particulate titanium dioxide as in Test Example 1) in castor oil, and the degree of odor denaturation was measured.
  • Test Example 2 The castor oil dispersions of Test Example 2 and Comparative Test Example 2 were stored in a 50° C. thermostat tank, and organoleptic evaluation was conducted for the degree of odor denaturation after 2 weeks.
  • the spherical composite powder obtained in Example 7 was strained through a 200 mesh sieve to obtain a spherical composite powder with particle sizes of 2 to 30 ⁇ m.
  • a powder friction tester Journal of Society of Powder Engineering vol. 21, No. 9, p. 565, 1984
  • a double-side tacky tape was plastered on an iron plate placed horizontally, a sample was placed thereon, then a load (5-70 g/cm 2 ) was applied on an attachment made of aluminum, and the shear stress when the attachment was moved right and left at a speed of 10 mm/sec. was measured, and the dynamic frictional coefficient was determined from the relationship between the load and the shear stress.
  • the spherical composite powder of the present invention can be seen to be spherical composite powder with a good slippage with a smaller frictional coefficient, compared with the simple powdery mixture of Comparative Example 5.
  • Example 7 In 1,000 ml of water, 10 g of aluminum powder with sizes of 0.1 ⁇ m or less and an average particle size of 0.08 ⁇ m was dispersed. Further, 30 g of Laponite XLG was dispersed to effect gelation. The gel was spray dried as in Example 7 to obtain 32 g of spherical composite powder containing the aluminum resin.
  • the composite powder was confirmed by scanning electron microscope observation that it is truly spherical and contains aluminum powder embedded extremely uniformly in the powder.
  • the spherical composite powder obtained in Example 10 dispersed at 10% by weight in castor oil, kneaded thoroughly on three rollers and then applied on a quartz plate by an applicator to a thickness of 5 ⁇ m, followed by measurement of the amount of UV-rays absorbed.
  • fine particulate titanium dioxide not applied with the composite powder formation of the present invention fine particulate titanium dioxide P-25; Degusa Co.
  • fine particulate titanium dioxide P-25 fine particulate titanium dioxide P-25; Degusa Co.
  • the fine particulate titanium dioxide not applied with the composite powder formation of the present invention was dispersed at 2.5% (the same as the amount of particulate titanium dioxide as in Test Example 1) in castor oil, and the amount of UV-rays absorbed was measured as in Test Example 2.
  • the spherical composite powder obtained in Test Example 1 was dispersed at 50% by weight in castor oil, and the degree of odor denaturation of castor oil was measured.
  • fine particulate titanium dioxide not applied with the composite powder formation of the present invention fine particulate titanium dioxide P-25; Degusa Co.
  • fine particulate titanium dioxide P-25 fine particulate titanium dioxide P-25; Degusa Co.
  • the fine particulate titanium dioxide not applied with the composite powder formation of the present invention was dispersed at 2.5% (the same as the amount of particulate titanium dioxide as in Test Example 2) in castor oil, and the degree of odor denaturation was measured.
  • Test Example 4 The castor oil dispersions of Test Example 4 and Comparative Test Example 4 were stored in a 50° C. thermostat tank, and an organoleptic evaluation was conducted for the degree of odor denaturation after 2 weeks.
  • the spherical composite powder obtained in Example 10 was strained through a 200 mesh sieve to obtain a spherical composite powder with particle sizes of 2 to 30 ⁇ m.
  • a powder friction tester Journal of Society of Powder Engineering vol. 21, No. 9, p. 565, 1984
  • a double-side tacky tape was plastered on an iron plate placed horizontally, a sample was placed thereon, then a load (5-70 g/cm 2 ) was applied on an attachment made of aluminum, the shear stress when the attachment was moved right and left at a speed of 10 mm/sec. was measured, and the dynamic frictional coefficient was determined from the relationship between the load and the shear stress.
  • the spherical composite powder of the present invention can be seen to be a spherical composite powder with a good slippage with a smaller frictional coefficient, compared with the simple powdery mixture of Comparative Example 6.
  • Example 10 In 1,000 ml of water was dispersed 10 g of aluminum powder with sizes of 0.1 ⁇ m or less and an average particle diameter of 0.08 ⁇ m. Further, 30 g of Laponite XLG was dispersed to effect gelation. The gel was spray dried as in Example 10 to obtain 32 g of a spherical composite powder containing aluminum powder. Further, the spherical powder was calcined at 600° C. for 2 hours. The composite powder was confirmed by a scanning electron microscope or EDX measurement to be truly spherical and contain the aluminum powder extremely uniformly dispersed in the powder.
  • Powders were respectively charged in a Henschel mixer, stirred uniformly and the remaining components then added and uniformly mixed.
  • the mixture was pulverized by an atomizer and molded in a midplate to obtain a powdery foundation.
  • Organoleptic evaluation was performed according to the five ranks of 1 to 5 shown below.
  • the powder was found to include 25% by weight of glycerine between layers, and the interlayer distance was found by X-ray diffraction to be expanded by about 4 ⁇ .
  • Example 15 In 1,000 ml of water were dissolved 10 g of glycerine and sodium hyaluronate, and further, 30 g of Laponite XLG was dispersed while stirring in the solution. The gel obtained was spray dried as in Example 15 to obtain 32 g of a spherical powder with entirely the same appearance as in Example 15.
  • Example 16 In 1,000 ml of water was dispersed 10 g of Laponite while stirring. The gel obtained was spray dried as in Example 16 to obtain 32 g of a spherical powder with entirely the same appearance as in Example 16.
  • Powders were respectively charged in a Henschel mixer, stirred uniformly and the remaining components then added and uniformly mixed.
  • the mixture was pulverized by an atomizer and molded in a midplate to obtain a powdery foundation.
  • Organoleptic evaluation was performed according to the five ranks of 1 to 5 shown below.
  • a lipstick was trial-produced by using the spherical powder of Example 16 according to the following formulated amounts (numerical values are in % by weight).
  • Waxes and oil components were charged in a kettle and melted by heating at 90° C. Further, pigments, perfume and spherical powder were added, and mixed by heating at 85° C. After degassing under a reduced pressure, the mixture was filled in a container, followed by solidification by cooling to obtain a lipstick.
  • the lipstick obtained was found to smoothly spread and according to the evaluation method as in Example 1, rated ⁇ in both good slippage and moistness.
  • Table 7 shows a list of spherical clay minerals prepared according to various conditions.
  • Laponite XLG, 30 g was dispersed while stirring in one liter of water.
  • the gel obtained was spray dried by a disc spray dryer at a disc rotational number of 20,000 rpm, an inlet air temperature of 200° C. and an exhaust temperature of 110° C. to obtain 24 g of a spherical powder of 2 to 10 ⁇ m.
  • Powders were respectively charged in a Henschel mixer, uniformly mixed and the remaining components then added and uniformly mixed.
  • the mixture was pulverized by an atomizer and molded in a midplate to obtain a powdery foundation.
  • the numerals in Table 9 are average scores of a panel of 20 members.
  • Oil components and waxes were melted by heating at 85° to 95° C., and powders were added and dispersed therein. The mixture was immediately degassed under a reduced pressure, transferred into a predetermined container, and solidified by cooling to obtain a lipstick.
  • Example 21 was found to be a lipstick with an extremely light spread, with the score by the use test in Table 2 being 4.2, and finished with a transparent look. On the other hand, Comparative Example 8 was slightly powdery with a heavy spread, and the score of useability was 2.1.
  • Pigments were mixed, and other components were added by melting with heating, followed by mixing and pulverization. This was molded in a midplate to obtain a press-shaped rouge.
  • Example 22 was found to be a rouge with an extremely good spread and finished with a transparent look without a powdery feeling.
  • Table 10 shows a list of spherical organic clay minerals prepared under various conditions.
  • the powder thus obtained maintained its original shape, and the interlayer distance was found by X-ray diffraction to be expanded by about 4 ⁇ in exactly the same manner as in the powder obtained in the (Preparation method) No. 1. Thus, glycerine was confirmed to be contained between the layers.
  • Powders were respectively charged into a Henschel mixer, uniformly stirred and the remaining components then added and uniformly mixed.
  • the mixture was pulverized by an atomizer and molded in a midplate to obtain a powdery foundation.
  • the numerals in Table 12 are average scores of a panel of 20 members.
  • the powdery foundation according to the present invention has a good slippage and excellent humectant property.
  • Oil components and waxes were melted by heating at 85°-95° C., and pigments were added and dispersed therein. The mixture was immediately degassed, transferred into a predetermined container and solidified by cooling to obtain a lipstick.
  • Example 24 was found to be a lipstick with an extremely light spread, with the score according to the use test in Example 12 being 4.2, and had a feeling of moistness.
  • Comparative Example 9 was found to have a slightly heavy spread, with the score being 2.0, and gave no feeling of moistness.
  • Pigments were mixed, and other components were added by melting with heating, followed by mixing and pulverization.
  • the mixture was molded in a midplate to obtain a press-shaped rouge.
  • Example 25 was found to have an extremely good spread, finished without a powdery feeling, and moistness was felt on the cheek.
  • an aerosol deodorant spray having the following composition was prepared.
  • the test method is as described below.
  • the test of the deodorant of the present invention was conducted by a panel of six healthy men aware of having an axillary odor.
  • the test product was directly applied on only the axillary odor site once in the morning and in the afternoon every day for 2 days, a total of 4 times.
  • the axillary odor site not applied with test product was called the control.
  • Judgement was conducted according to the five judgement standards shown below, namely:
  • Example 26 In place of the composite powder used in Example 26, as powdery mixture obtained by simply mixing 0.3 g of fine zinc oxide and 0.9 g of Laponite XLG was used to prepare an aerosol deodorant spray in the same manner as in Example 25.
  • the results of the deodorizing test conducted with the deodorant sprays of Example 26 and Comparative Example 10 are shown in Table 14. Thus, it can be understood that the composite powder of the present invention has a greater deodorant effect than when the respective components are individually formulated.
  • g of a composite powder was obtained from 80 g of Smecton SA (produced by Kunimine Kogyo Co.) and 20 g of fine zinc oxide.
  • Smecton SA produced by Kunimine Kogyo Co.

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  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
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  • Dispersion Chemistry (AREA)
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US07/538,595 1986-07-24 1990-06-14 Spherical clay mineral powder, process for production thereof and composition containing the same Expired - Lifetime US5165915A (en)

Applications Claiming Priority (14)

Application Number Priority Date Filing Date Title
JP61-174578 1986-07-24
JP61174578A JPH0696447B2 (ja) 1986-07-24 1986-07-24 複合粉体及びその製造法
JP61188333A JPS6343665A (ja) 1986-08-11 1986-08-11 消臭剤
JP61-188333 1986-08-11
JP61194493A JPH075292B2 (ja) 1986-08-20 1986-08-20 球状粘土鉱物及びその製造法
JP61-194493 1986-08-20
JP19449486A JPS6351310A (ja) 1986-08-20 1986-08-20 球状の粘土鉱物を配合した化粧料
JP61-194494 1986-08-20
JP61-208624 1986-09-04
JP20862486A JPH0662288B2 (ja) 1986-09-04 1986-09-04 球状の有機複合粘土鉱物及びその製造法
JP61209161A JPH0717371B2 (ja) 1986-09-05 1986-09-05 球状の有機複合粘土鉱物及びその製造法
JP20916086A JPS6366111A (ja) 1986-09-05 1986-09-05 球状の有機複合粘土鉱物を配合した化粧料
JP61-209161 1986-09-05
JP61-209160 1986-09-05

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Cited By (57)

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US5376698A (en) * 1993-09-21 1994-12-27 The Mearl Corporation Polyolefin compositions containing coated mica particles to prevent yellowing and methods therefore
US5378388A (en) * 1993-06-25 1995-01-03 The Procter & Gamble Company Granular detergent compositions containing selected builders in optimum ratios
US5431911A (en) * 1993-06-21 1995-07-11 Reynolds; Diane S. Skin treatment composition
DE19504899A1 (de) * 1994-09-26 1996-03-28 Nat Inst Res Inorganic Mat Poröser Körper aus Polysaccharid oder Polysaccharid-Ton-Komposit und Verfahren für dessen Herstellung
US5518728A (en) * 1994-08-08 1996-05-21 L'oreal S.A. Cosmetic compositions for non-white pigmented skin
US5538728A (en) * 1989-10-19 1996-07-23 Shiseido Company, Ltd. Hydrophilic polymer-silicate mineral complex material and use thereof
US5551975A (en) * 1994-06-23 1996-09-03 J. M. Huber Corporation Structured pigment compositions, methods for preparation and use
US5562763A (en) * 1992-04-07 1996-10-08 Merck Patent Gesellschaft Mit Beschrankter Haftung Process for the preparation of composite pigments
US5618342A (en) * 1991-12-04 1997-04-08 Merck Patent Gesellschaft Mit Beschrankter Haftung Pigment preparation
US5651962A (en) * 1995-09-21 1997-07-29 Kligerman; Myron R. Dry pre-shaving composition
US5667580A (en) * 1994-09-14 1997-09-16 Ciba-Geigy Corporation Pigment compositions
US5753242A (en) * 1994-05-02 1998-05-19 Shiseido Company, Ltd. External skin treatment composition
US5785959A (en) * 1996-08-16 1998-07-28 Revlon Consumer Products Corporation Nail strengthening compositions and a method for strengthening nails
US5800818A (en) * 1995-12-12 1998-09-01 Laboratoires De Biologie Vegetale Yves Rocher Mixture comprising plant extracts for moisturizing the upper layers of the epidermis
US5807540A (en) * 1995-05-05 1998-09-15 L'oreal Nail varnish composition comprising a crosslinked polyester
US5882662A (en) * 1997-05-09 1999-03-16 Avon Products, Inc. Cosmetic compositions containing smectite gels
US5882683A (en) * 1995-01-09 1999-03-16 Mitsubishi Pencil Kabushiki Kaisha Stick cosmetics and production process for the same
US5904918A (en) * 1996-11-04 1999-05-18 L'oreal S.A. Cosmetic powder composition
US6080390A (en) * 1997-08-27 2000-06-27 Revlon Consumer Products Corporation Moisturizing cosmetic stick compositions
US6140303A (en) * 1997-09-08 2000-10-31 Haarmann & Reimer Gmbh Fragrance-containing preparation
US6197284B1 (en) * 1992-08-06 2001-03-06 Kanebo, Ltd. Lipcolor composition
US6207174B1 (en) * 1997-12-01 2001-03-27 Shiseido Company, Ltd. Composite powder and coloring containing the same
US6235277B1 (en) * 1995-09-13 2001-05-22 Marcel Jean Deodorant granulates for ashtrays
US6355280B1 (en) * 2000-02-28 2002-03-12 I.M.S. Cosmetics Composition for reducing cell apoptosis containing avocado and soybean lipid unsaponifiables
US6479040B1 (en) * 2001-02-06 2002-11-12 Coty Inc. Cosmetic formulation
US6517863B1 (en) 1999-01-20 2003-02-11 Usbiomaterials Corporation Compositions and methods for treating nails and adjacent tissues
US6562323B1 (en) * 1999-03-29 2003-05-13 Catalysts & Chemicals Industries Co., Ltd. Composite powder, cosmetic and paint with the composite powder blended therein
US20030144161A1 (en) * 2002-01-29 2003-07-31 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Detergent compositions
US20030176309A1 (en) * 2002-01-29 2003-09-18 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Detergent compositions
US20040009246A1 (en) * 1999-02-24 2004-01-15 Allan Taylor Preparation for regulating lower bowel function
US20040091628A1 (en) * 2000-11-03 2004-05-13 The Procter & Gamble Company Methods of fragrancing a surface
US20040110652A1 (en) * 2002-12-05 2004-06-10 Unilever Home & Personal, Care Usa Division Of Conopco, Inc. Detergent compositions
US20040146617A1 (en) * 1998-10-27 2004-07-29 Schrader Lawrence E Compositions and methods for suppressing cracking and water loss from cherries
US6857224B1 (en) 1998-10-27 2005-02-22 Washington State University Research Foundation Use of clay and lipid formulations to protect horticultural crops from sunburn and insect damage
US20050113255A1 (en) * 1998-10-27 2005-05-26 Washington State University Research Foundation Use of lipid formulations to protect horticultural crops
US7189407B2 (en) 1998-09-21 2007-03-13 Shiseido Co., Ltd. Composition for external use
US20070190097A1 (en) * 1998-10-27 2007-08-16 Schrader Lawrence E Compositions and Methods for Suppressing Cracking and Water Loss from Cherries
US20080119519A1 (en) * 2005-02-21 2008-05-22 Nanohybrid Co., Ltd. Base Forming Drug-Layered Silicate Hybrid Containing Basic Polymer and its Synthesis Method
US20080161431A1 (en) * 2006-12-29 2008-07-03 Korwin-Edson Michelle L Room temperature crosslinked foam
US20080161430A1 (en) * 2006-12-29 2008-07-03 Korwin-Edson Michelle L Room temperature crosslinked foam
US20080161432A1 (en) * 2006-12-29 2008-07-03 Korwin-Edson Michelle L Room temperature crosslinked foam
US20080160203A1 (en) * 2006-12-29 2008-07-03 O' Leary Robert J Spray-in latex foam for sealing and insulating
US20080161433A1 (en) * 2006-12-29 2008-07-03 Korwin-Edson Michelle L Room temperature crosslinked foam
US20080281006A1 (en) * 2007-05-09 2008-11-13 O Leary Robert J One-part non-toxic spray foam
US20090107066A1 (en) * 2007-10-31 2009-04-30 O'leary Robert Wall construction air barrier system
US20090111902A1 (en) * 2007-10-25 2009-04-30 Korwin-Edson Michelle L Room temperature crosslinked material
US20100175810A1 (en) * 2006-12-29 2010-07-15 Korwin-Edson Michelle L Room temperature crosslinked foam
US20100189908A1 (en) * 2006-12-29 2010-07-29 Olang Fatemeh N Formulation method for plural component latex- foam
US20110123717A1 (en) * 2006-12-29 2011-05-26 O'leary Robert J Two part spray foam using a blowing agent as a plasticizer and a room temperature crosslinking agent
US20110224317A1 (en) * 2009-01-19 2011-09-15 Owens Corning Intellectual Capital, Llc Spray foams with fine particulate blowing agent
CN104059393A (zh) * 2014-05-27 2014-09-24 池州凯尔特纳米科技有限公司 一种分散均匀的复合改性碳酸钙及其制备方法
JP2015151357A (ja) * 2014-02-13 2015-08-24 日本メナード化粧品株式会社 複合粉体
US9228074B2 (en) 2012-05-07 2016-01-05 Burgess Pigment Company Spray-dried, hydrous, kaolin clay and methods of making same
CN106619159A (zh) * 2017-01-10 2017-05-10 韩后化妆品股份有限公司 提高油包水型乳霜粘度稳定性的方法
US11096960B2 (en) * 2003-12-02 2021-08-24 Core Intellectual Properties Holdings, Llc Mineral, nutritional, cosmetic, pharmaceutical, and agricultural compositions and methods for producing the same
WO2023135170A1 (fr) * 2022-01-13 2023-07-20 Givaudan Sa Composition
WO2023186618A1 (fr) 2022-03-28 2023-10-05 Unilever Ip Holdings B.V. Composition à stabilité et qualité sensorielle accrues

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US6352699B1 (en) * 1997-04-04 2002-03-05 L'oreal Cosmetic or dermatological composition forming, on a keratin substrate, a film in cross-linked hybrid material
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UY33555A (es) * 2011-08-12 2013-02-28 Jeporu S A Pintura no tóxica apta para expresión artística
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US3439088A (en) * 1964-06-16 1969-04-15 Exxon Research Engineering Co Cosmetic preparations-wax rouge and foundation make-up
JPS5141443A (ja) * 1974-10-03 1976-04-07 Kobayashi Kose Co Keshoryo
US3998973A (en) * 1975-04-07 1976-12-21 R. T. Vanderbilt Company, Inc. Thickening composition
JPS5232024A (en) * 1975-09-05 1977-03-10 Pola Chem Ind Inc Method for the preparation of pigment
US4431673A (en) * 1980-05-02 1984-02-14 Revlon, Inc. Cosmetic compositions
JPS60228406A (ja) * 1984-04-27 1985-11-13 Pola Chem Ind Inc 化粧料
US4659571A (en) * 1985-03-20 1987-04-21 Nl Industries, Inc. Compressed powder formulation containing organophilic clay and a process for making the formulation
US4783333A (en) * 1986-03-17 1988-11-08 Charles Of The Ritz Group, Ltd. Cosmetic containing color particles
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JPH01111367A (ja) * 1987-10-26 1989-04-28 Fujitsu Ltd Ｃｍｏｓ半導体装置

Cited By (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5538728A (en) * 1989-10-19 1996-07-23 Shiseido Company, Ltd. Hydrophilic polymer-silicate mineral complex material and use thereof
US5618342A (en) * 1991-12-04 1997-04-08 Merck Patent Gesellschaft Mit Beschrankter Haftung Pigment preparation
US5562763A (en) * 1992-04-07 1996-10-08 Merck Patent Gesellschaft Mit Beschrankter Haftung Process for the preparation of composite pigments
US6197284B1 (en) * 1992-08-06 2001-03-06 Kanebo, Ltd. Lipcolor composition
US5431911A (en) * 1993-06-21 1995-07-11 Reynolds; Diane S. Skin treatment composition
US5378388A (en) * 1993-06-25 1995-01-03 The Procter & Gamble Company Granular detergent compositions containing selected builders in optimum ratios
US5376698A (en) * 1993-09-21 1994-12-27 The Mearl Corporation Polyolefin compositions containing coated mica particles to prevent yellowing and methods therefore
US5753242A (en) * 1994-05-02 1998-05-19 Shiseido Company, Ltd. External skin treatment composition
US5551975A (en) * 1994-06-23 1996-09-03 J. M. Huber Corporation Structured pigment compositions, methods for preparation and use
US5518728A (en) * 1994-08-08 1996-05-21 L'oreal S.A. Cosmetic compositions for non-white pigmented skin
US5667580A (en) * 1994-09-14 1997-09-16 Ciba-Geigy Corporation Pigment compositions
DE19504899A1 (de) * 1994-09-26 1996-03-28 Nat Inst Res Inorganic Mat Poröser Körper aus Polysaccharid oder Polysaccharid-Ton-Komposit und Verfahren für dessen Herstellung
DE19504899B4 (de) * 1994-09-26 2006-04-20 National Institute For Research In Inorganic Materials, Tsukuba Poröser Körper aus Polysaccharid oder Polysaccharid-Ton-Komposit und Verfahren für dessen Herstellung
US6228501B1 (en) 1994-09-26 2001-05-08 National Institute For Research In Inorganic Materials Porous body of polysaccharide or polysaccharide-clay composite, and process for its production
US5882683A (en) * 1995-01-09 1999-03-16 Mitsubishi Pencil Kabushiki Kaisha Stick cosmetics and production process for the same
US5807540A (en) * 1995-05-05 1998-09-15 L'oreal Nail varnish composition comprising a crosslinked polyester
US6235277B1 (en) * 1995-09-13 2001-05-22 Marcel Jean Deodorant granulates for ashtrays
US5651962A (en) * 1995-09-21 1997-07-29 Kligerman; Myron R. Dry pre-shaving composition
US5800818A (en) * 1995-12-12 1998-09-01 Laboratoires De Biologie Vegetale Yves Rocher Mixture comprising plant extracts for moisturizing the upper layers of the epidermis
US5785959A (en) * 1996-08-16 1998-07-28 Revlon Consumer Products Corporation Nail strengthening compositions and a method for strengthening nails
US5904918A (en) * 1996-11-04 1999-05-18 L'oreal S.A. Cosmetic powder composition
US5882662A (en) * 1997-05-09 1999-03-16 Avon Products, Inc. Cosmetic compositions containing smectite gels
US6080390A (en) * 1997-08-27 2000-06-27 Revlon Consumer Products Corporation Moisturizing cosmetic stick compositions
US6140303A (en) * 1997-09-08 2000-10-31 Haarmann & Reimer Gmbh Fragrance-containing preparation
US6207174B1 (en) * 1997-12-01 2001-03-27 Shiseido Company, Ltd. Composite powder and coloring containing the same
US7189407B2 (en) 1998-09-21 2007-03-13 Shiseido Co., Ltd. Composition for external use
US20050113255A1 (en) * 1998-10-27 2005-05-26 Washington State University Research Foundation Use of lipid formulations to protect horticultural crops
US20070190097A1 (en) * 1998-10-27 2007-08-16 Schrader Lawrence E Compositions and Methods for Suppressing Cracking and Water Loss from Cherries
US7222455B2 (en) 1998-10-27 2007-05-29 Washington State University Research Foundation Compositions and methods for suppressing cracking and water loss from cherries
US20040146617A1 (en) * 1998-10-27 2004-07-29 Schrader Lawrence E Compositions and methods for suppressing cracking and water loss from cherries
US6857224B1 (en) 1998-10-27 2005-02-22 Washington State University Research Foundation Use of clay and lipid formulations to protect horticultural crops from sunburn and insect damage
US6517863B1 (en) 1999-01-20 2003-02-11 Usbiomaterials Corporation Compositions and methods for treating nails and adjacent tissues
US20040009246A1 (en) * 1999-02-24 2004-01-15 Allan Taylor Preparation for regulating lower bowel function
US6916495B2 (en) * 1999-02-24 2005-07-12 Allan Taylor Preparation for regulating lower bowel function
US6562323B1 (en) * 1999-03-29 2003-05-13 Catalysts & Chemicals Industries Co., Ltd. Composite powder, cosmetic and paint with the composite powder blended therein
US6355280B1 (en) * 2000-02-28 2002-03-12 I.M.S. Cosmetics Composition for reducing cell apoptosis containing avocado and soybean lipid unsaponifiables
US20040091628A1 (en) * 2000-11-03 2004-05-13 The Procter & Gamble Company Methods of fragrancing a surface
US7041337B2 (en) * 2000-11-03 2006-05-09 The Procter & Gamble Company Methods of fragrancing a surface
US6479040B1 (en) * 2001-02-06 2002-11-12 Coty Inc. Cosmetic formulation
US6649151B2 (en) 2001-02-06 2003-11-18 Coty Inc. Cosmetic formulation
US7030077B2 (en) * 2002-01-29 2006-04-18 Unilever Home And Personal Care Usa, A Division Of Conopco, Inc. Detergent compositions
US7033983B2 (en) * 2002-01-29 2006-04-25 Unilever Home and Personal Care USA a division of Conopco, Inc. Detergent compositions
US20030176309A1 (en) * 2002-01-29 2003-09-18 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Detergent compositions
US20030144161A1 (en) * 2002-01-29 2003-07-31 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Detergent compositions
US20040110652A1 (en) * 2002-12-05 2004-06-10 Unilever Home & Personal, Care Usa Division Of Conopco, Inc. Detergent compositions
US7033984B2 (en) * 2002-12-05 2006-04-25 Unilever Home And Personal Care Usa Division Of Conopco, Inc. Detergent compositions
US11096960B2 (en) * 2003-12-02 2021-08-24 Core Intellectual Properties Holdings, Llc Mineral, nutritional, cosmetic, pharmaceutical, and agricultural compositions and methods for producing the same
US20080119519A1 (en) * 2005-02-21 2008-05-22 Nanohybrid Co., Ltd. Base Forming Drug-Layered Silicate Hybrid Containing Basic Polymer and its Synthesis Method
US20080161432A1 (en) * 2006-12-29 2008-07-03 Korwin-Edson Michelle L Room temperature crosslinked foam
US9714331B2 (en) 2006-12-29 2017-07-25 Owens Corning Intellectual Capital, Llc Room temperature crosslinked foam
US20080160203A1 (en) * 2006-12-29 2008-07-03 O' Leary Robert J Spray-in latex foam for sealing and insulating
US20080161433A1 (en) * 2006-12-29 2008-07-03 Korwin-Edson Michelle L Room temperature crosslinked foam
US20080161431A1 (en) * 2006-12-29 2008-07-03 Korwin-Edson Michelle L Room temperature crosslinked foam
US9868836B2 (en) 2006-12-29 2018-01-16 Owens Corning Intellectual Capital, Llc Room temperature crosslinked foam
US20080161430A1 (en) * 2006-12-29 2008-07-03 Korwin-Edson Michelle L Room temperature crosslinked foam
US20100175810A1 (en) * 2006-12-29 2010-07-15 Korwin-Edson Michelle L Room temperature crosslinked foam
US20100189908A1 (en) * 2006-12-29 2010-07-29 Olang Fatemeh N Formulation method for plural component latex- foam
US20110123717A1 (en) * 2006-12-29 2011-05-26 O'leary Robert J Two part spray foam using a blowing agent as a plasticizer and a room temperature crosslinking agent
US8875472B2 (en) 2006-12-29 2014-11-04 Owens Corning Intellectual Capital, Llc Room temperature crosslinked foam
US8779016B2 (en) * 2006-12-29 2014-07-15 Owens Corning Intellectual Capital, Llc Spray-in latex foam for sealing and insulating
US20080281006A1 (en) * 2007-05-09 2008-11-13 O Leary Robert J One-part non-toxic spray foam
US20090111902A1 (en) * 2007-10-25 2009-04-30 Korwin-Edson Michelle L Room temperature crosslinked material
US8209915B2 (en) 2007-10-31 2012-07-03 Owens Corning Intellectual Capital, Llc Wall construction air barrier system
US20090107066A1 (en) * 2007-10-31 2009-04-30 O'leary Robert Wall construction air barrier system
US20110224317A1 (en) * 2009-01-19 2011-09-15 Owens Corning Intellectual Capital, Llc Spray foams with fine particulate blowing agent
US9228074B2 (en) 2012-05-07 2016-01-05 Burgess Pigment Company Spray-dried, hydrous, kaolin clay and methods of making same
JP2015151357A (ja) * 2014-02-13 2015-08-24 日本メナード化粧品株式会社 複合粉体
CN104059393A (zh) * 2014-05-27 2014-09-24 池州凯尔特纳米科技有限公司 一种分散均匀的复合改性碳酸钙及其制备方法
CN104059393B (zh) * 2014-05-27 2015-07-01 池州凯尔特纳米科技有限公司 一种分散均匀的复合改性碳酸钙及其制备方法
CN106619159A (zh) * 2017-01-10 2017-05-10 韩后化妆品股份有限公司 提高油包水型乳霜粘度稳定性的方法
CN106619159B (zh) * 2017-01-10 2019-10-11 韩后化妆品股份有限公司 提高油包水型乳霜粘度稳定性的方法
WO2023135170A1 (fr) * 2022-01-13 2023-07-20 Givaudan Sa Composition
WO2023186618A1 (fr) 2022-03-28 2023-10-05 Unilever Ip Holdings B.V. Composition à stabilité et qualité sensorielle accrues

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EP0277244A1 (fr) 1988-08-10
EP0277244A4 (fr) 1989-01-19
WO1988000572A1 (fr) 1988-01-28
DE3750576D1 (de) 1994-10-27
EP0277244B1 (fr) 1994-09-21
DE3750576T2 (de) 1995-04-27

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